An Open-Label, Multicenter Study to Evaluate the Pharmacokinetics, Safety, and Efficacy of Glecaprevir/Pibrentasvir in Pediatric Subjects with Genotypes 1-6 Chronic Hepatitis C Virus (HCV) Infection
| Sponsor: |
AbbVie, Inc. |
| Enrolling: |
Male and Female Patients |
| Study Length: |
160 Weeks |
| Clinic Visits: |
13 |
| IRB Number: |
AAAR2252 |
| U.S. Govt. ID: |
NCT03067129 |
| Contact: |
Danilo Gamino: 212-305-6758 / dg3031@cumc.columbia.edu |
Open-labeled hepatitis C pediatric treatment trial with a two drug direct acting viral oral combination (already approved in adults) across all genotypes for naive or treatment experienced subjects.
This study is closed
Investigator
Steven Lobritto, MD
| Has your child been diagnosed with Hepatitis C virus? |
Yes |
No |
| Has your child tested positive for Hepatitis B? |
Yes |
No |